Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1450703683
ANOS1
1.000 0.160 X 8533018 missense variant T/C snv 1.9E-05 1
rs587780174
CHEK2
0.827 0.360 22 28695239 frameshift variant A/- delins 4.4E-05 5.6E-05 7
rs131821
NCAPH2
0.851 0.160 22 50511648 intron variant T/-;TT;TTT;TTTT delins 4
rs138740
TOM1
0.882 0.160 22 35303589 intron variant C/T snv 0.51 3
rs710190
CBX7
0.925 0.200 22 39131785 3 prime UTR variant T/C snv 0.48 2
rs12158877
CBX7
1.000 0.160 22 39153421 upstream gene variant T/G snv 0.45 1
rs138747
TOM1
1.000 0.160 22 35304495 intron variant A/C;T snv 1
rs139371
CBX7
1.000 0.160 22 39123191 intron variant T/C;G snv 1
rs139385
CBX7
1.000 0.160 22 39134127 non coding transcript exon variant C/A snv 0.46 1
rs139402
CBX7
1.000 0.160 22 39150140 intron variant T/C snv 0.43 1
rs139426 1.000 0.160 22 39164661 intergenic variant G/A snv 0.26 1
rs34101942 1.000 0.160 22 39167907 intergenic variant -/A delins 0.68 1
rs713841
CBX7
1.000 0.160 22 39133024 3 prime UTR variant A/G snv 0.67 1
rs877529
CBX7
1.000 0.160 22 39146287 intron variant G/A snv 0.43 1
rs961773676
SGSM3
1.000 0.160 22 40409505 missense variant G/A snv 1
rs2834167
IL10RB
0.752 0.360 21 33268483 missense variant A/G snv 0.33 0.25 11
rs765506701
IL10RB
1.000 0.160 21 33288130 missense variant G/A;C snv 4.0E-06; 8.0E-06 1
rs6066835
PREX1
1.000 0.160 20 48738472 intron variant T/C snv 9.0E-02 1
rs6071887 1.000 0.160 20 39992814 intergenic variant A/G;T snv 1
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs759412116
ERCC2
0.581 0.640 19 45352210 missense variant C/G;T snv 4.0E-06; 6.0E-05 55
rs2043211
CARD8
0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs73005220
CIB3
0.851 0.160 19 16161878 intron variant A/G snv 3.9E-02 4
rs2903754
ANKRD27
0.925 0.200 19 32600776 intron variant C/T snv 0.62 2
rs11086029
KLF2
1.000 0.160 19 16327850 3 prime UTR variant T/A snv 0.78 1